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FDA 510(k)

CRITIC-AID WOUND DRESSING

K-Number: K912506 · 1992-03-02

ApplicantSween Corp.
Decision Date1992-03-02
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CRITIC-AID WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Sween Corp.. It received FDA 510(k) clearance on 1992-03-02 under 510(k) number K912506. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRITIC-AID WOUND DRESSING?

CRITIC-AID WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1992-03-02. The listed applicant is Sween Corp.. The 510(k) number is K912506.

When did CRITIC-AID WOUND DRESSING receive FDA 510(k) clearance?

CRITIC-AID WOUND DRESSING received FDA 510(k) clearance on 1992-03-02, under 510(k) number K912506.

Who is the listed applicant for CRITIC-AID WOUND DRESSING?

The FDA 510(k) record lists Sween Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRITIC-AID WOUND DRESSING?

The FDA product code for CRITIC-AID WOUND DRESSING is KMF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Sween Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K926389SWEEN WOUND CARE-COLLAGEN WOUND DRESSINGK840723SWEEN-A-PEEL PERISTOMAL WAFERSK810846SWEEN UNIVERSAL BED RAIL PADS

Related Devices (Code: KMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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